Vegetable Vigra Nutritional Supplement Recall [US]

US FlagUS/Silver Spring: Vegetable Vigra brand Nutritional Supplement Recall [US]Natures Supplement, Inc. recalls an estimated 260 bottles of Vegetable Vigra brand Nutritional Supplements due to suspected undeclared Sildenafil an FDA approved drug for the treatment of Erectile Dysfunction, all serious health and safety hazards. FDA: http://ht.ly/N6YG30fnc98

Direct link: https://www.fda.gov/Safety/Recalls/ucm576834.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Supplements are subject to this recall:

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AMPT Coffee Recall [US]

US FlagUS/Silver Spring: US Food and Drug AdministrationThe AMPT Life, LLC recalls all batch/lots of AMPT Coffee due to suspected presence of Sildenafil and Tadalafil, active ingredients in two FDA-approved prescription drugs as well as undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention. FDA: http://ht.ly/SFrx30ebqMl

Direct link: https://www.fda.gov/Safety/Recalls/ucm569558.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following beverage is subject to this recall:

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Caverflo Natural Herbal Coffee Recall [US]

US FlagUS/Silver Spring: Caverflo Natural Herbal Coffee Recall [US]Caverflo.com recalls all batch/lots of Caverflo branded Natural Herbal Coffee due to suspected presence of Sildenafil and Tadalafil, active ingredients in two FDA-approved prescription drugs as well as undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention. The company has received a report of one (1) death linked to drinking this Coffee product. FDA: http://ht.ly/zhKU30cemKo

Direct link: https://www.fda.gov/Safety/Recalls/ucm560680.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following beverage is subject to this recall:

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Ultimate Body Tox PRO Supplement Recall [US]

US FlagUS/Silver Spring: FDA Logo BlueUltimate Body–Tox recalls certain batch/lots of Ultimate Body Tox PRO Supplements due to undeclared Sibutramine, a controlled substance that was removed from the US market in October 2010 for safety reasons and a serious health hazard. FDA: http://ht.ly/cI1A306NvTJ

Direct link: http://www.fda.gov/Safety/Recalls/ucm531190.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Supplements are subject to this recall:

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Megajex Male Sex Supplement Recall [US]

US FlagUS/Silver Spring: FDA Logo BlueMS Bionic, Inc. recalls all batch/lots of Megajex Natural Male Sex Enhancer Supplements due to undeclared Tadalafil and Sildenafil, FDA-approved prescription drugs used as treatment for male Erectile Dysfunction. FDA: http://ht.ly/ggc0306IE3i

Direct link: http://www.fda.gov/Safety/Recalls/ucm531176.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Supplement is subject to this recall:

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Black Ant, Mojo Risen Supplement Recall Expands [US]

US FlagUS/Silver Spring: 3474 - BlackAntDietary SupplementEugene Oregon expands its existing recall of African Black Ant, Black Ant and Mojo Risen Dietary Supplements to include all lot numbers due to undeclared drug ingredients, a serious health and safety hazard. FDA: http://ht.ly/xtpPs

Direct link: http://www.fda.gov/Safety/Recalls/ucm399144.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following dietary supplements are subject to this recall: Continue reading

Human Science Foundation Pro ArthMax Recall [US]

US FDA RecallUS/Silver Spring: Human Science Foundation recalls some Pro ArthMax due to undeclared drug hazard. FDA: http://ht.ly/sAo8H2998 - HumanScienceFoundationProArthMax

Direct link: http://www.fda.gov/Safety/Recalls/ucm381494.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplements are subject to this recall: Continue reading

Midwest Wholesale Dietary Supplement Recall [US]

US FDA RecallUS/Silver Spring: Midwest Wholesale recalls various Dietary Supplements due to undeclared drugs, a health hazard. These Supplements are sold under the Boost Ultra, Magic for Men, “New” Extenze, New XZen Platinum, Sexy Monkey, Triple MiracleZen Platinum and XZone Gold brands. FDA: http://ht.ly/svi6DMidwest Boost Supplement

Direct link: http://www.fda.gov/Safety/Recalls/ucm381299.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplements are subject to this recall: Continue reading

VitaliKOR Fast Acting Dietary Supplement Recall [US]

US FDA RecallUS/Silver Spring: Vitality Research Labs recalls some VitaliKOR Fast Acting Dietary Supplements due to undeclared drug hazard, specifically Vardenafil and Tadalafil. FDA: http://ht.ly/r1qf6

VitaliKOR Dietary Supplements

Direct link: http://www.fda.gov/Safety/Recalls/ucm375104.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following dietary supplements are subject to this recall: Continue reading

Creafuse Powder Dietary Supplement Recall [US]

US FDA RecallUS/Silver Spring: GE Pharma recalls some Creafuse Powder Dietary Supplements due to undeclared drug hazard. FDA: http://ht.ly/p5cuZ 

Direct link: http://www.fda.gov/Safety/Recalls/ucm368314.htm

Additional information:Creafuse Powder Dietary Supplement
The US Food and Drug Administration (“FDA”) reports the following Supplements are subject to this recall:

  • Creafuse Powder Grape Lot# GE4568, packaged in a white, 600 gram container with an expiration date of 2/2015
  • Creafuse Powder Fruit Punch Lot #GE4570, packaged in a white, 600 gram container with an expiration date of 2/2015

According to the FDA, both recalled Dietary Supplements contain 1,3 dimethylamylamine (“DMAA”). DMAA is commonly used as a stimulant, pre-workout and weight loss ingredient in dietary supplement products. The FDA has warned that DMAA is potentially dangerous to health. Ingestion of DMAA can elevate blood pressure and lead to cardiovascular problems. A number of adverse effects associated with DMAA containing dietary supplements have been reported to the FDA. The FDA has also warned that DMAA is not a dietary ingredient and thus, is not Dietary Supplement Health and Education Act (DSHEA) compliant.

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Tranquility Nutritional Supplement Recall [US]

US FDA RecallUS/Silver Spring: Health and Beyond LLC recalls some Tranquility Nutritional Supplements due to undeclared drug hazard. FDA: http://ht.ly/nKVL6

Direct link: http://www.fda.gov/Safety/Recalls/ucm364227.htm

Additional information:Tranquility Nutritional Supplements
The US Food and Drug Administration (“FDA”) reports the Tranquility Nutritional Supplements are sold as a sleep product and are packaged in a white bottle with 30 pills per bottle with lot numbers 36678 and 36680. The affected product in the Tranquility lots include the expiration date of “9/15”.

According to the FDA, the recalled Tranquility Nutritional Supplements contain two undeclared drugs: a trace of Doxepin which is a pharmaceutical for sleep, and Chlorpormazine, a drug used to control psychotic disorders.

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Recalls Direct RIN: 2013-2369
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Purity First Nutritional Supplement Recall [US]

US FDA RecallUS/Silver Spring: PFDA Logourity First Health Products recalls some Healthy Life Chemistry B-50, Multi-Mineral and Vitamin C Products due to undeclared drugs hazard. FDA: http://ht.ly/nydNy

Direct link: http://www.fda.gov/Safety/Recalls/ucm363374.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Drugs are subject to this recall:

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Herbal Give Care Nutritional Supplement Recall [US]

US FDA RecallUS/Silver Spring: Herbal Give Care recalls some Esbelin Siloutte Nutritional Supplements due to undeclared drug hazard, specifically,  Sibutramine, N-Desmethylsibutramine and N-di-Desmethylsibutramine. FDA: http://ht.ly/ndsj2

Direct link:  http://www.fda.gov/Safety/Recalls/ucm361950.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Drugs are subject to this recall:

  • Esbelin Siloutte Herbal Blend with L-Carnitine: this Supplement is marketed to help normalize nervous appetite as well as prevent fat accumulation and fluid retention in tissues. The Esbelin Siloutte Herbal Blend with L-Carnitine (30 Capsules) is packaged in a white plastic bottle with a screw cap containing 30 capsules per bottle. All lots of this product are being recalled. This Supplement was distributed nationwide to retail customers and via the internet. The UPC code for this product is 7502011000060.
  • Esbelin Siloutte Te: this Supplement is marketed as a fat burner, in that it is claimed to remove the fat stored in the body, thereby achieving elimination of the fat through the urine and preventing its accumulation. The product is also marketed to promote the proper functioning of the consumer’s digestive system. This product is packaged in a gold resealable foil pouch; the product does not have the unit size labeled. The recall includes all lots of the Esbelin Siloutte Te. This Supplement was also distributed nationwide to retail customers and via the internet. The UPC code for this product is 7562684652553.

According to the FDA, both Supplements pose dangers to consumers because Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of Coronary Artery Disease, Congestive Heart Failure, Arrhythmias or Stroke.

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Recalls Direct RIN: 2013-2297
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Bethel 30 Weight Loss Pill Recall [US]

US FDA RecallUS/Silver Spring: Bethel Nutritional Consulting recalls some Bethel 30 Weight Loss Pills due to undeclared drug hazard. FDA: http://ht.ly/lVWvk

Direct link: http://www.fda.gov/Safety/Recalls/ucm356233.htm

Additional information:
Bethel Weight Loss Front of BottleThe US Food and Drug Administration (“FDA”) reports some Bethel 30 Weight Loss Pills tested positive for Sibutramine and Phenolphthalein, two undeclared drugs. Sibutramine is a controlled substance removed from the market in October 2010 for safety reasons. The FDA has not approved Bethel 30, Green Capsules as drugs; therefore the safety and effectiveness of this product is unknown.Bethel Weight Loss Bottle Label

According to the US FDA, these products may pose a threat to consumers because Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. This product may also interact, in life-threatening ways, with other medications a consumer may be taking.

Please note: other Dietary Supplements manufactured by this company have been recalled. To see all recalls and notifications related to this manufacturer, please search for “Bethel Nutritional” using the Search Box at the top of this page.

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Additional information about this recall:
Recalls Direct RIN: 2013-2114
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SexVoltz, Velextra, Amerect Dietary Supplement Recall [US]

United StatesUS/Silver Spring: BeaMonstar Products recalls some SexVoltz, Velextra and Amerect Dietary Supplements due to undeclared drug hazard. FDA: http://ht.ly/kPjaMSexVoltz Nutritional Supplement

Direct link: http://www.fda.gov/Safety/Recalls/ucm351162.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports that testing by the US FDA found BeaMonstar Products’ SexVoltz, Velextra and Amerect Dietary Supplements contain or have the potential to contain an analogue of Tadalafil, Continue reading

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